Neoadjuvant hormonal therapy prior to radical prostatectomy: the European experience.

Molecular urology Pub Date : 2000-01-01
F M Debruyne, W P Witjes
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Abstract

Background and purpose: Neoadjuvant hormonal therapy (NHT) has been used for more than a decade for prostate cancer, but the results of clinical trials are only now becoming available, and the value of the treatment is not yet clear. The authors reviewed the results of the European randomized trials to increase our understanding of the role of this treatment.

Patients and methods: We report the results of 402 patients with prostate cancer (220 clinical stage T(2) and 182 clinical T(3) tumor), of whom 192 were randomly assigned to NHT using an LHRH analog (goserelin) plus flutamide for a period of 3 months (NHT) and 210 underwent radical prostatectomy only (RP).

Results: "Pathologic downstaging" occurred in 15% and 7% of the NHT and the RP group, respectively (P < 0.01). Fifty of the 189 patients in the NHT group (26%) and 68 of the 209 patients in the RP group (33%) developed disease progression, as determined by rising serum prostate specific antigen (PSA) concentration. Regarding local disease progression, the advantage for the use of NHT approached but did not reach statistical significance:18 of 189 patients (10%) in the NHT group and 33 of 209 patients (16%) in the RP group (P = 0. 07).

Conclusions: Although there was a trend in favor of the NHT group with respect to the number of patients with PSA progression and the number with local disease progression, it did not reach statistical significance. These results may be attributable to a true lack of benefit of adjuvant hormonal ablation or to a lack of statistical power to demonstrate a difference in a subset of patients who might benefit from this therapy.

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根治性前列腺切除术前的新辅助激素治疗:欧洲的经验。
背景和目的:新辅助激素治疗(NHT)用于前列腺癌已有十多年的历史,但临床试验的结果直到现在才开始可用,治疗的价值尚不清楚。作者回顾了欧洲随机试验的结果,以增加我们对这种治疗作用的理解。患者和方法:我们报告了402例前列腺癌患者(220例临床T(2)期和182例临床T(3)期肿瘤)的结果,其中192例随机分配到使用LHRH类似物(戈舍雷林)加氟他胺的NHT组,为期3个月(NHT), 210例仅行根治性前列腺切除术(RP)。结果:NHT组和RP组病理降分期发生率分别为15%和7% (P < 0.01)。NHT组189例患者中有50例(26%)和RP组209例患者中有68例(33%)出现疾病进展,这是通过血清前列腺特异性抗原(PSA)浓度升高来确定的。对于局部疾病进展,使用NHT的优势接近但未达到统计学意义:NHT组189例患者中有18例(10%),RP组209例患者中有33例(16%)(P = 0。07年)。结论:虽然在PSA进展的患者数量和局部疾病进展的患者数量上有NHT组优势的趋势,但没有达到统计学意义。这些结果可能是由于确实缺乏辅助激素消融的益处,或者是由于缺乏统计能力来证明可能从这种治疗中受益的一部分患者的差异。
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